Author: Vigil, Adam; Martinez, Osvaldo; Chua, Mark A; GarcÃa-Sastre, Adolfo
                    Title: Recombinant Newcastle disease virus as a vaccine vector for cancer therapy  Cord-id: lalsa4ie  Document date: 2008_11_1
                    ID: lalsa4ie
                    
                    Snippet: Naturally occurring strains of Newcastle disease virus (NDV) are currently being investigated in multiple clinical trials for oncolytic cancer therapy in the US and abroad. We have previously reported for the first time the development of recombinant NDVs designed for enhanced cancer therapeutic efficacy. Specifically, we have shown that NDV engineered to express IL-2 generates a robust therapeutic response associated with increased tumor specific T cell infiltration after intratumoral administr
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Naturally occurring strains of Newcastle disease virus (NDV) are currently being investigated in multiple clinical trials for oncolytic cancer therapy in the US and abroad. We have previously reported for the first time the development of recombinant NDVs designed for enhanced cancer therapeutic efficacy. Specifically, we have shown that NDV engineered to express IL-2 generates a robust therapeutic response associated with increased tumor specific T cell infiltration after intratumoral administration in mice. We have now demonstrated that this therapeutic response is dependent on T cells and we have investigated the potential to focus the NDV-induced immune response towards a tumor-associated antigen (TAA) in order to further enhance the inherent therapeutic efficacy of NDV. We found that intratumoral treatments of tumor-bearing mice with recombinant NDV expressing a model TAA elicited an enhanced tumor specific response, resulting in a significant increase in the number of complete tumor regressions as compared to control NDV. Additionally, coadministration of NDV expression a model TAA with NDV expressing IL-2 enhanced the TAA directed response and led to more complete tumor regressions. Our results show that TAA directed immunotherapy by oncolytic recombinant NDV alone or in combination with IL-2 results in an enhanced therapeutic efficacy and warrant consideration in the development of cancer therapies based on the use of oncolytic NDV.
 
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